The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α^3.7 Deletion Defect

Cornelis L. Harteveld Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333, AL Leiden, The Netherlands

Kirsten Van Lom Department of Hematology, Erasmus Medical Center, GD Rotterdam, The Netherlands

Encarna B. Gomez Garcia Department of Hematology, Erasmus Medical Center, GD Rotterdam, The Netherlands

Peter van Delft Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333, AL Leiden, The Netherlands

Piero C. Giordano Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333, AL Leiden, The Netherlands

References

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The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α^3.7 Deletion Defect

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The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α3.7 Deletion Defect

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The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α^3.7 Deletion Defect